Ankleshwar, Gujarat, India · On-site
Implement and monitor EHS policies, procedures, and safe work practices across the plant. Ensure compliance with applicable statutory requirements, including Factories Act, Pollution Control Board regulations, Hazardous …
Skills: EHS Policy Implementation, Statutory Compliance, Safety Inspections, Permit-to-Work, Lockout-Tagout
Ankleshwar, Gujarat, India · On-site
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
Skills: Production Monitoring, cGMP Compliance, Documentation, Equipment Calibration, Safety Management
Ankleshwar, Gujarat, India · On-site
Perform chemical analysis of raw materials, intermediates, APIs, stability samples, and finished products using approved analytical methods. Operate and maintain analytical instruments such as HPLC, GC, UV-Visible Spectr…
Skills: Chemical Analysis, HPLC, GC, UV-Visible Spectrophotometry, FTIR
Ankleshwar, Gujarat, India · On-site
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
Skills: Production Monitoring, cGMP Compliance, BPR Documentation, Equipment Calibration, Safety Management
Ankleshwar, Gujarat, India · On-site
Perform analysis of raw materials, intermediates, finished products, in-process samples, and stability samples as per approved specifications and test methods. Operate and maintain analytical instruments such as HPLC, GC…
Skills: HPLC, GC, UV-Visible Spectrophotometry, FTIR, Dissolution Testing
Ankleshwar, Gujarat, India · On-site
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
Skills: Production Management, cGMP Compliance, Documentation, Safety Management, Quality Control
Ankleshwar, Gujarat, India · On-site
Documentation: • To prepare SOP’s/ URS/ BPR/ Protocol/ Investigation report for regulatory compliance as per available procedure/practice. • Ensure that all documents / records required for Regulatory Compliance are main…
Skills: SOP Preparation, Regulatory Compliance, GDP, GMP Compliance, CAPA
Ankleshwar, Gujarat, India · On-site
Execute manufacturing activities for API intermediates and finished active pharmaceutical ingredients as per approved Batch Manufacturing Records (BMRs), SOPs, and production plans. Operate and monitor process equipment …
Skills: API Manufacturing, cGMP, Good Documentation Practices, Process Equipment Operation, Line Clearance
Ankleshwar, Gujarat, India · On-site
Process Development: • Conduct laboratory experiments & trials to modify processes develop shorter processes to reduce present cost. • Send sample to QC of studied experiment. • Contact QC dept. to solicit support & foll…
Skills: Process Development, Laboratory Experiments, Sample Analysis, Data Generation, Vendor Qualification
Ankleshwar, Gujarat, India · On-site
• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packing materials/intermed…
Skills: HPLC Analysis, GLP Compliance, CFR 21 Part 11, LIMS, Stability Study
Ankleshwar, Gujarat, India · On-site
Execute API manufacturing activities as per Batch Manufacturing Records (BMR) and approved Standard Operating Procedures (SOPs). Operate and monitor reactors, centrifuges, dryers, filters, blenders, micronizers, and othe…
Skills: API Manufacturing, cGMP, GDP, Data Integrity, Equipment Operation
Ankleshwar, Gujarat, India · On-site
• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packing materials/intermed…
Skills: HPLC Analysis, GLP Compliance, CFR 21 Part 11, LIMS, Stability Study
Ankleshwar, Gujarat, India · On-site
Perform analysis of raw materials, intermediates, APIs, stability samples, and finished products using HPLC. Operate, calibrate, and maintain HPLC systems as per SOPs. Prepare mobile phases, reagents, standard solutions,…
Skills: HPLC, Analytical Method Validation, Method Verification, Method Transfer, GMP
Ankleshwar, Gujarat, India · On-site
• To ensure the timely sampling and testing of purified water, Process and finish product samples. • To ensure timely regeneration and maintenance of the Culture • To ensure the media preparation as per the analysis plan…
Skills: Microbiology Testing, Environmental Monitoring, LIMS, GLP, GMP
Ankleshwar, Gujarat, India · On-site
• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packing materials/intermed…
Skills: HPLC Analysis, GLP Compliance, CFR 21 Part 11, LIMS, Stability Study
Ankleshwar, Gujarat, India · On-site
Principal Tasks &Responsibilities • Work allocation for sampling , analysis of finish products, returned goods and review of analytical data generated through LIMS / modules and report to Section Head / or HOD - QC. • Re…
Skills: Quality Control, LIMS, SAP, Analytical Method Validation, Regulatory Compliance
Ankleshwar, Gujarat, India · On-site
Participate in customer, regulatory, and internal audits including USFDA, MHRA, WHO-GMP, EDQM, and other global regulatory inspections. Provide analytical data and laboratory documentation during inspections. Ensure audi…
Skills: Regulatory Audits, Analytical Documentation, cGMP, GLP, Data Integrity
Ankleshwar, Gujarat, India · On-site
• To ensure cGMP compliance at manufacturing facility [PR, PR (SRP), Quality units, HR, EHS, ST, EG departments] as well as to ensure the whether they are following the standard procedures. • Responsible to ensure online…
Skills: cGMP Compliance, Data Integrity, Line Clearance, Quality Assurance, CAPA
Ankleshwar, Gujarat, India · On-site
Review and approve batch manufacturing records (BMR), batch packaging records (BPR), logbooks, and analytical reports. Perform line clearance activities before and after manufacturing operations. Monitor and verify compl…
Skills: cGMP, GDP, Data Integrity, SOP Review, Line Clearance
Ankleshwar, Gujarat, India · On-site
Plan and execute daily, weekly, and monthly API production activities as per the production schedule. Ensure adherence to cGMP, SOPs, BMR/BPR, and regulatory requirements. Monitor manufacturing processes, batch yields, c…
Skills: API Production, cGMP Compliance, Production Planning, Team Supervision, CAPA Implementation
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Implement and monitor EHS policies and safe work practices to ensure compliance with statutory environmental and safety regulations. Coordinate the operation of treatment plants and conduct safety inspections, incident investigations, and emergency response training.
The candidate must be able to manage statutory records and licenses while ensuring the safe handling of hazardous chemicals. Experience in coordinating with multiple departments to execute safe work procedures and support regulatory audits is required.
Implement and monitor EHS policies, procedures, and safe work practices across the plant.
Ensure compliance with applicable statutory requirements, including Factories Act, Pollution Control Board regulations, Hazardous Waste Management Rules, MSIHC Rules, PESO requirements, and other environmental and safety regulations.
Conduct daily plant safety inspections and identify unsafe acts and unsafe conditions.
Ensure effective implementation of Permit-to-Work (PTW), Lockout-Tagout (LOTO), confined space entry, hot work, work at height, and electrical safety procedures.
Monitor the safe handling, storage, and disposal of hazardous chemicals, solvents, and waste.
Coordinate operation and compliance activities related to Effluent Treatment Plant (ETP), Sewage Treatment Plant (STP), Air Pollution Control Systems (APCS), and hazardous waste management.
Conduct incident, accident, near-miss, and unsafe condition investigations and implement corrective and preventive actions (CAPA).
Organize safety induction programs, toolbox talks, emergency response training, and mock drills.
Ensure statutory inspections, testing, and certification of fire protection systems, pressure vessels, lifting tools, and safety equipment.
Monitor usage and compliance of Personal Protective Equipment (PPE) across all departments.
Maintain statutory records, licenses, permits, safety reports, and EHS documentation.
Coordinate with Production, Engineering, QA, QC, Warehouse, and contractors to ensure safe execution of work.
Support internal, customer, and regulatory EHS audits and ensure timely closure of observations.
Promote 5S, behavioral safety, and continuous improvement initiatives.
The Care Continues...
Founded by Shri I.A. Modi, Cadila Pharmaceuticals Ltd. is one of the largest privately held pharmaceutical companies in India, headquartered at Ahmedabad, in the State of Gujarat. Over the last seven decades, the company has been developing and manufacturing pharmaceutical products in India and selling and distributing these in over hundred other countries around the world. Focused strongly on Innovation and Research, the company is present in more than forty-five therapeutic areas spread across twelve specialities, including cardiovascular, gastrointestinal, analgesics, haematinics, anti-infectives and antibiotics, respiratory agents, antidiabetics and immunologicals. At Cadila Pharmaceuticals, Research and Development is at the core of all its initiatives, be it Biotechnology, APIs, Formulations, Plant Tissue Culture or Phytochemistry. More than 300 scientists in its various Research and Development setups reinforce the competitiveness of research in the therapeutic areas which have high unmet medical needs. Cadila Pharmaceuticals Excellence in manufacturing facilities is central to Cadila Pharmaceuticals. The company’s formulations manufacturing plant at Dholka near Ahmedabad, Gujarat is spread over hundred acres of land. This state-of-the- art facility is not only impressive in size, but is also USFDA approved. The second formulations manufacturing facility is located at Samba in Jammu and Kashmir. The facility meets most of the stringent quality standards across the globe to produce tablets, capsules, soft and hard gelatin capsules, liquids and orals. Two Active Pharmaceutical Ingredient (API) manufacturing units at Ankleshwar, Gujarat manufacture a wide range of APIs and intermediates including many USFDA-certified products. The company has strong foothold in the African continent through its formulation manufacturing facility at Addis Ababa in Ethiopia. For more information visit: https://www.cadilapharma.com/
Offices: Sarkhej-Dholka Road, Bhat, Ahmedabad, Gujarat 382210, IN · Survey No. 1389, Trasad Road, Dholka, Ahmedabad, Gujarat 387 810, IN · 294, GIDC Estate, Ankleshwar, Gujarat, IN · Survey No. 342, Nani Kadi, Taluka Kadi, Dist. Mehsana, Gujarat, IN · Survey No. 342, Nani Kadi, Taluka Kadi, Dist. Mehsana, Gujarat, IN
There are currently 165 open manufacturing positions in Ankleshwar, India listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Cadila Pharmaceuticals Limited, Zentiva, Asian Paints, Indorama Ventures: Indovinya, among others. Browse the listings above to see every active employer.
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